Last Updated: September 28, 2026

Drug Master Files for: ETOPOSIDE PHOSPHATE

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ETOPOSIDE PHOSPHATE Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
10191	I	II	4/13/1993	PHARMACEUTICAL FACTORY SHANGHAI INSTITUTE PHARMACEUTICAL INDUSTRY	ETOPOSIDE
10476	A	II	9/17/1993	NIPPON KAYAKU CO LTD	ETOPOSIDE PHOSPHATE
10642	A	II	12/30/1993	CIPLA LTD	ETOPOSIDE USP
13986	I	II	2/17/1999	RP SCHERER CANADA INC	ETOPOSIDE 50MG SOFT-GELATIN CAPSULE
24332	I	II	10/8/2010	QILU PHARMACEUTICAL CO LTD	ETOPOSIDE (NON-STERILE API)
4385	I	II	11/6/1981	SANDOZ LTD PHARMACEUTICAL DIV CHEMICAL DEVELOPMENT	ETOPOSIDE (VP 16-213) (ETHYLIDENE)
8647	A	II	7/2/1990	JIANGSU HENGRUI MEDICINE CO LTD	ETOPOSIDE USP
>DMF No.	>Status	>Type	>Submission Date	>Holder	>Subject

Drug Master File Glossary

STATUS OF DMFS

A = Active. This means that the DMF was found acceptable for filing, administratively, and is up-to-date.
I = Inactive
N = Not an assigned number
P = DMF Pending Filing Review

TYPES OF DMFs

Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)
Type II Drug Substance, Drug Substance Intermediate, and Material Used in Their Preparation, or Drug Product
Type III Packaging Material
Type IV Excipient, Colorant, Flavor, Essence, or Material Used in Their Preparation
Type V FDA Accepted Reference Information

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